Please provide your email address to receive an email when new articles are posted on . Of the nearly 783,000 Americans with kidney failure, approximately 500,000 of these patients require ...

A Chesterfield medical device company has earned an FDA breakthrough designation for its vein dilation system designed to ...

Amplifi Vascular, Inc., a developer of solutions for hemodialysis vascular access, announced it has been granted Breakthrough ...

Amplifi Vascular, Inc., has been granted Breakthrough Device Designation and Category B assignment from the Centers for Medicare & Medicaid Services (CMS) for the Amplifi Vein Dilation System. This ...

Amplifi Vascular announced that it received breakthrough device designation for its Amplifi Vein Dilation System.

In 2016, the American College of Emergency Physicians (ACEP) issued a policy statement advocating a new safety goal for vascular access: the “one-stick standard.” To help clinicians achieve it, ACEP ...

Dublin, Dec. 10, 2025 (GLOBE NEWSWIRE) -- The "Vascular Access Device - Market Insights, Competitive Landscape, and Market Forecast - 2032" has been added to ResearchAndMarkets.com's offering. This ...

We were unable to process your request. Please try again later. If you continue to have this issue please contact customerservice@slackinc.com. Healio has compiled a list of the most-read vascular ...

Intraosseous (IO) vascular access has emerged as a critical technique in emergency medicine, offering rapid and reliable delivery of fluids and medications when traditional intravenous (IV) access ...

BILLERICA, Mass.--(BUSINESS WIRE)--Access Vascular, Inc. (AVI), a leader in tackling critical vascular access challenges with its advanced hydrophilic biomaterial technology, today announced a ...

BILLERICA, Mass.--(BUSINESS WIRE)--Access Vascular, Inc. (AVI), a leader in tackling critical vascular access challenges with its advanced hydrophilic biomaterial technology, today announced that its ...